| Journal Articles: 55 results |
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Pyrolysis of Aryl Sulfonate Esters in the Absence of Solvent: E1 or E2? A Puzzle for the Organic Laboratory John J. Nash, Marnie A. Leininger, and Kurt Keyes An aryl sulfonate ester is synthesized and then pyrolyzed at reduced pressure. The volatile products are analyzed using gas chromatography to determine whether the thermal decomposition occurs via an E1 or E2 mechanism. Nash, John J.; Leininger, Marnie A.; Keyes, Kurt. J. Chem. Educ. 2008, 85, 552.
Alkenes |
Carbocations |
Elimination Reactions |
Gas Chromatography |
Mechanisms of Reactions |
Synthesis
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A Discovery-Based Experiment Involving Rearrangement in the Conversion of Alcohols to Alkyl Halides Richard A. Kjonaas and Ryand J. F. Tucker This article reports a discovery-based experiment in which students convert three alcohols to alkyl halides under acidic conditions and record the 13C NMR spectrum in each case. By comparing the number of resonances observed with the number of resonances predicted for each possible product, students draw several conclusions about the resulting rearrangement. Kjonaas, Richard A.; Tucker, Ryand J. F. J. Chem. Educ. 2008, 85, 100.
Alcohols |
Carbocations |
Gas Chromatography |
NMR Spectroscopy |
Nucleophilic Substitution
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Dynamic Stereochemistry: A Simple Approach To Delineating Relative Configuration Dipak K. Mandal A simple approach is presented for delineating relative stereochemistry of the product in reactions involving stereogenic center(s). Mandal, Dipak K. J. Chem. Educ. 2007, 84, 274.
Chirality / Optical Activity |
Diastereomers |
Enantiomers |
Molecular Properties / Structure |
Stereochemistry
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Regioselective Synthesis of a Stereodefined Heterocyclic Push–Pull Alkene. 1H NMR Studies and Two-Dimensional TLC Illustrating Z/E Isomerization Rade Markovi, Marija Baranac, Vesna Jovanovi, and Zdravko Dambaski Facile and direct regioselective synthesis of the 4-oxothiazolidine derivative from inexpensive chemicals as an example of kinetic versus thermodynamic control is described. Markovi, Rade; Baranac, Marija; Jovanovi, Vesna; Dambaski, Zdravko. J. Chem. Educ. 2004, 81, 1026.
Heterocycles |
Alkenes |
Stereochemistry |
Synthesis |
NMR Spectroscopy
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Pressure Dependence of Gas-Phase Reaction Rates Stéphanie de Persis, Alain Dollet, and Francis Teyssandier This article is intended to show that only simple concepts are required to qualitatively explain and describe the pressure dependence of gas-phase reaction rates. de Persis, Stéphanie; Dollet, Alain; Teyssandier, Francis. J. Chem. Educ. 2004, 81, 832.
Qualitative Analysis |
Gases |
Kinetics |
Mechanisms of Reactions
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The Monosodium Glutamate Story: The Commercial Production of MSG and Other Amino Acids Addison Ault Examples of the industrial synthesis of pure amino acids are presented. The emphasis is on the synthesis of (S)-glutamic acid and, to a lesser extent, (S)-lysine and (R,S)-methionine. These amino acids account for about 90% of the total world production of amino acids. Ault, Addison. J. Chem. Educ. 2004, 81, 347.
Amino Acids |
Biotechnology |
Chirality / Optical Activity |
Consumer Chemistry |
Enzymes |
Natural Products |
Stereochemistry |
Synthesis |
Food Science
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Spiral Puzzle for Organic Chemistry Students Ender Erdik Puzzle to review organic reactions and their reagents. Erdik, Ender. J. Chem. Educ. 2003, 80, 428.
Synthesis |
Learning Theories |
Enrichment / Review Materials |
Addition Reactions |
Alkylation |
Electrophilic Substitution |
Elimination Reactions |
Reactions |
Nucleophilic Substitution |
Mechanisms of Reactions |
Grignard Reagents
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The Importance of Non-Bonds in Coordination Compounds Michael Laing Significance of noncovalent interactions in determining the structure and behavior of coordination compounds. Laing, Michael. J. Chem. Educ. 2001, 78, 1400.
Noncovalent Interactions |
Coordination Compounds |
Kinetics |
Stereochemistry |
Molecular Properties / Structure
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Synthesis and Use of Jacobsen's Catalyst: Enantioselective Epoxidation in the Introductory Organic Laboratory John Hanson Laboratory series to introduce students to an important synthetic method and many common techniques used in running reactions, purifying products, and characterizing compounds. Hanson, John. J. Chem. Educ. 2001, 78, 1266.
Catalysis |
Chirality / Optical Activity |
Synthesis |
Organometallics |
Stereochemistry |
Epoxides |
Enantiomers |
Aromatic Compounds
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Catalytic Asymmetric Epoxidation Using a Fructose-Derived Catalyst Andy Burke, Patrick Dillon, Kyle Martin, and T. W. Hanks Modern epoxidation methods are able to create two adjacent stereocenters with very high enantioselectivity. Opening of the epoxides with nucleophiles permits rapid entry into complex organic systems, making this powerful synthetic methodology one of the fundamental reactions in organic synthesis. Burke, Andy; Dillon, Patrick; Martin, Kyle; Hanks, Timothy W. J. Chem. Educ. 2000, 77, 271.
Catalysis |
NMR Spectroscopy |
Stereochemistry |
Enantiomers
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Chart for Deciding Mechanism for Reaction of Alkyl Halide with Nucleophile/Base McClelland, Bruce W. The decision chart offered here is based upon the well-known and accepted characteristics of the reaction system mechanisms described in typical introductory organic chemistry textbooks. McClelland, Bruce W. J. Chem. Educ. 1994, 71, 1047.
Mechanisms of Reactions |
Nucleophilic Substitution
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Photometric Determination of the Rate Expression for MnO4- Mediated Organic Oxidations Crouch, R. David Photometric procedure for studying the kinetics of the MnO4- mediated oxidation of mandelic acid in KOH. Crouch, R. David J. Chem. Educ. 1994, 71, 597.
Rate Law |
Oxidation / Reduction |
Photochemistry |
Kinetics
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The aromatic substitution game Zanger, Murray; Gennaro, Alfonso R.; McKee, James R. This paper describes a game used to bring attention to the need for students to reconsider substitution theories learned in earlier chapters. Zanger, Murray; Gennaro, Alfonso R.; McKee, James R. J. Chem. Educ. 1993, 70, 985.
Nucleophilic Substitution |
Synthesis
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Information sources for organic chemistry, 3 Somerville, Arleen N. This article is the third in a series that provides ready-to-use lecture material about organic chemistry information sources, a chart that links sources with questions which is suitable for distribution to students, and a set of practice questions. Somerville, Arleen N. J. Chem. Educ. 1992, 69, 379.
Solutions / Solvents
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Thermal decomposition of a natural manganese dioxide: A laboratory experiment for undergraduate students Puerta, M. C.; Valerga, P. This is a very instructive experiment that combines experimental work, theoretical discussion, and literature investigation. Puerta, M. C.; Valerga, P. J. Chem. Educ. 1990, 67, 344.
Thermodynamics |
Kinetics |
Molecular Properties / Structure |
Thermal Analysis |
Solid State Chemistry
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Critical behavior in the solubility of ionic compounds Gillispie, Gregory D. The process of an ionic compound dissolving in a pure solvent is a convenient way to introduce Debye-Huckel activity coefficients. Gillispie, Gregory D. J. Chem. Educ. 1990, 67, 143.
Solutions / Solvents |
Ionic Bonding |
Electrolytic / Galvanic Cells / Potentials
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A note on the meaning of the electroneutrality condition for solutions Sastre, M.; Santaballa, J. A. It is necessary to make clear to students that the Nernst-Plank macroscopic electrical neutrality condition is not a fundamental law of nature, though it is an excellent approximation to reality. Sastre, M.; Santaballa, J. A. J. Chem. Educ. 1989, 66, 403.
Solutions / Solvents |
Electrochemistry
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Solving differential equations in kinetics by using power series Hughes, Elvin, Jr. This article describes an approach for solving eq 2, a differential equation that arises in the discussion of a set of consecutive chemical reactions that are outlined in eq 1. Hughes, Elvin, Jr. J. Chem. Educ. 1989, 66, 46.
Kinetics |
Chemometrics
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Two working models for the SN2 mechanism Anderson, Martin M. Design of an articulated physical model demonstrating the mechanism of the SN2 reaction. Anderson, Martin M. J. Chem. Educ. 1987, 64, 1023.
Nucleophilic Substitution |
Mechanisms of Reactions |
Molecular Modeling
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Kinetics of oxidation of bromcresol green Pickering, Miles; Heiler, David Study of the bleaching of bromcresol green by hypochlorite. Pickering, Miles; Heiler, David J. Chem. Educ. 1987, 64, 81.
Kinetics |
Oxidation / Reduction |
Dyes / Pigments |
Acids / Bases |
Mechanisms of Reactions
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Kinetic stability, kinetic control, and descriptive inorganic chemistry Webb, Michael J. Examples, demonstrations, and laboratory work involving kinetic stability and kinetic control in inorganic chemistry. Webb, Michael J. J. Chem. Educ. 1984, 61, 988.
Kinetics |
Descriptive Chemistry
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Aromatic substitution reactions: when you've said ortho, meta, and para you haven't said it all Traynham, James G. The author presents a range of examples for nucleophilic, electrophilic, and free-radical reactions where the ipso is an important, predominant, or even exclusive site of reaction. Traynham, James G. J. Chem. Educ. 1983, 60, 937.
Nucleophilic Substitution |
Electrophilic Substitution |
Free Radicals |
Diastereomers |
Stereochemistry |
Reactions
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Organosilicon chemistry. Part II West, Robert; Barton, Thomas J. Stereochemistry and reaction mechanisms, reactive intermediates, bioactive organosilanes, organosilanes in organic synthesis, and sources of silicon compounds. West, Robert; Barton, Thomas J. J. Chem. Educ. 1980, 57, 334.
Molecular Properties / Structure |
Stereochemistry |
Mechanisms of Reactions |
Reactive Intermediates
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A time-lag method for second-order kinetics Espenson, James H. Circumvents the need for a reliable endpoint for kinetic investigations of second-order reactions. Espenson, James H. J. Chem. Educ. 1980, 57, 160.
Kinetics
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Computation of the number of isomers of coordination compounds containing different monodentate ligands Chung, Chung-Sun
Chung, Chung-Sun J. Chem. Educ. 1979, 56, 398.
Chemometrics |
Molecular Properties / Structure |
Coordination Compounds |
Stereochemistry |
Diastereomers
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Phase transfer catalysis. Part II: Synthetic applications Gokel, George W.; Weber, William P. In this month's continuation of an article, the authors have catalogued a number of illustrative examples so that the range of applicability of phase transfer catalysis will be. Gokel, George W.; Weber, William P. J. Chem. Educ. 1978, 55, 429.
Phases / Phase Transitions / Diagrams |
Catalysis |
Aromatic Compounds |
Organometallics |
Nucleophilic Substitution |
Synthesis |
Esters |
Oxidation / Reduction |
Alkylation
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Purple benzene: Solubilization of anions in organic solvents Herriott, Arthur W. Demonstrates the preference of a typical salt for solution in water rather than nonpolar benzene; a quaternary ammonium salt, though soluble in water, is more soluble in benzene. Herriott, Arthur W. J. Chem. Educ. 1977, 54, 229.
Aromatic Compounds |
Precipitation / Solubility |
Solutions / Solvents |
Aqueous Solution Chemistry |
Molecular Properties / Structure
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Selective solubility: "Like dissolves like" Smith, Wayne L. Azobenzene is a better analog of DDT than iodine in demonstrating the pesticide's solubility in fatty tissue. Smith, Wayne L. J. Chem. Educ. 1977, 54, 228.
Precipitation / Solubility |
Solutions / Solvents |
Lipids
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Nucleophilic substitution reactions at secondary carbon atoms. A modification of accepted views Raber, Douglas J.; Harris, J. Milton Considers reaction mechanisms that are intermediate between SN1 and SN2 and the possible role of ion pairs. Raber, Douglas J.; Harris, J. Milton J. Chem. Educ. 1972, 49, 60.
Nucleophilic Substitution |
Mechanisms of Reactions
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Reaction mechanisms in organic chemistry. Concerted reactions Caserio, Marjorie C. Examines displacement and elimination, cyclization, and rearrangement reactions, as well as theoretical considerations and generalized selection rules. Caserio, Marjorie C. J. Chem. Educ. 1971, 48, 782.
Mechanisms of Reactions |
Reactions |
Nucleophilic Substitution |
Elimination Reactions
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Hydrolysis of benzenediazonium ion Sheats, John E.; Harbison, Kenneth G. Presents a more convenient approach to studying the kinetics of the hydrolysis of benzenediazonium ion. Sheats, John E.; Harbison, Kenneth G. J. Chem. Educ. 1970, 47, 779.
Aromatic Compounds |
Nucleophilic Substitution |
Kinetics
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Donor-acceptor interactions in organic chemistry Sunderwirth, S. G. The purpose of this article is to aid teachers in making even more effective use of theoretical considerations in teaching organic chemistry; the primary objective is to emphasize the underlying principles that are common to the following four basic types of reactions: substitution, addition, elimination, and rearrangement. Sunderwirth, S. G. J. Chem. Educ. 1970, 47, 728.
Reactions |
Mechanisms of Reactions |
Addition Reactions |
Elimination Reactions |
Nucleophilic Substitution
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The rearrangement of diazotized 4-bromobenzophenone hydrazone: A stereospecific reaction Hawbeker, Byron L. This procedure involves the synthesis of hydrazone and its subsequent diazotization / rearrangement to produce an anilide. Hawbeker, Byron L. J. Chem. Educ. 1970, 47, 218.
Reactions |
Stereochemistry |
Molecular Properties / Structure |
Aromatic Compounds |
Mechanisms of Reactions |
Synthesis
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Encounters and slow reactions Langford, Copper H. This paper reviews the formation of a metal ion and a ligand in a mechanistic language, as much derived from the collision theory as from transition state theory. Langford, Copper H. J. Chem. Educ. 1969, 46, 557.
Aqueous Solution Chemistry |
Metals |
Kinetics |
Mechanisms of Reactions |
Coordination Compounds |
Solutions / Solvents
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Kinetics of fast brominations: A potentiometric study Burgess, A. E.; Latham, J. L. Demonstrates that the kinetics of fast reactions such as the bromination of phenols in aqueous solution are easily determined by a simple potentiometric technique. Burgess, A. E.; Latham, J. L. J. Chem. Educ. 1969, 46, 370.
Kinetics |
Electrochemistry |
Rate Law
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Probabilistic derivation of the kinetic rate equations Lee, Tieh-Sheng; Kuffner, Roy J. The use of the probabilistic approach is readily applicable to reaction kinetics if one considers the probability of the survival of the reactant molecule instead of the survival of a radioactive nucleus. Lee, Tieh-Sheng; Kuffner, Roy J. J. Chem. Educ. 1968, 45, 430.
Kinetics
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Bimolecular nucleophilic displacement reactions Edwards, John O. The bimolecular nucleophilic displacement reaction is important and should be included in any detailed discussion of kinetics and mechanism at an early undergraduate level. Edwards, John O. J. Chem. Educ. 1968, 45, 386.
Reactions |
Nucleophilic Substitution |
Kinetics |
Mechanisms of Reactions
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Conformational analysis and chemical reactivity Idoux, John P. Uses acyclic chemistry to illustrate important concepts regarding conformational analysis and chemical reactivity. Idoux, John P. J. Chem. Educ. 1967, 44, 495.
Conformational Analysis |
Stereochemistry |
Diastereomers
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Substitution reactions in octahedral complexes Banerjea, D. Commentary on the cited article by one of the authors that article referenced. Banerjea, D. J. Chem. Educ. 1967, 44, 485.
Coordination Compounds |
Nucleophilic Substitution
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Determination of glucose: A kinetics experiment for the analytical course Toren, E. Clifford, Jr. This determination of glucose demonstrates both kinetic and enzymatic methods of analysis. Toren, E. Clifford, Jr. J. Chem. Educ. 1967, 44, 172.
Quantitative Analysis |
Carbohydrates |
Kinetics |
Enzymes
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Substitution reactions in octahedral complexes Jones, G. R. H. Examines the possibility of direct substitution, in aqueous solution, of a ligand in an octahedral complex by a nucleophile other than water or OH-. Jones, G. R. H. J. Chem. Educ. 1966, 43, 657.
Coordination Compounds |
Mechanisms of Reactions |
Aqueous Solution Chemistry |
Nucleophilic Substitution |
Transition Elements |
Metals
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On the spatial arrangement of atoms in nitrogen-containing molecules Hantzsch, A.; Werner, A. Reprint of Alfred Werner's inaugural dissertation on the one hundredth anniversary of his winning of the first Nobel Prize in chemistry. Hantzsch, A.; Werner, A. J. Chem. Educ. 1966, 43, 156.
Stereochemistry
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Reaction mechanisms in organic chemistry. I. The experimental approach Caserio, Marjorie C. Reviews a variety of method that may be employed to determine the mechanism of organic reactions. Caserio, Marjorie C. J. Chem. Educ. 1965, 42, 570.
Reactions |
Mechanisms of Reactions |
Reactive Intermediates |
Kinetics |
Nucleophilic Substitution |
Addition Reactions |
Elimination Reactions
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The effect of structure on chemical and physical properties of polymers Price, Charles C. Suggests using polymers to teach the effect of changes in structure on chemical reactivity, the effect of structure on physical properties, the role of catalysts, and the basic principles of a chain reaction mechanism. Price, Charles C. J. Chem. Educ. 1965, 42, 13.
Physical Properties |
Molecular Properties / Structure |
Polymerization |
Kinetics |
Reactions |
Catalysis |
Mechanisms of Reactions
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A second order kinetics experiment Teerlink, Wilford J.; Asay, Jeanette; Sugihara, James M. Investigates the nucleophilic displacement reaction of ethyl p-toluenesulfonate by iodide in acetone. Teerlink, Wilford J.; Asay, Jeanette; Sugihara, James M. J. Chem. Educ. 1964, 41, 161.
Kinetics |
Nucleophilic Substitution
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Nucleophilic reactions at trigonally bonded carbon Cash, R. Vincent Examines the mechanisms of nucleophilic displacement reactions, nucleophilic addition reactions, and nucleophilic addition with elimination, all at trigonally bonded carbon. Cash, R. Vincent J. Chem. Educ. 1964, 41, 108.
Nucleophilic Substitution |
Reactions |
Mechanisms of Reactions |
Addition Reactions |
Elimination Reactions
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The stereochemistry of complex inorganic compounds Busch, Daryle H. Examines optical activity, absolute configuration, stereospecificity, linkage isomers, electronic isomers, and template reactions. Busch, Daryle H. J. Chem. Educ. 1964, 41, 77.
Stereochemistry |
Coordination Compounds |
Crystal Field / Ligand Field Theory |
Chirality / Optical Activity |
Stereochemistry |
Molecular Properties / Structure
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Three-dimensional effects in biochemistry Ingraham, Lloyd L. Explores stereospecificity and stereoselectivity; rigidity requirements; steric effects; and stereospecificity when not required mechanistically. Ingraham, Lloyd L. J. Chem. Educ. 1964, 41, 66.
Molecular Properties / Structure |
Catalysis |
Enzymes |
Molecular Recognition |
Mechanisms of Reactions |
Stereochemistry |
Chirality / Optical Activity |
Enantiomers
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Crystal field theory and substitution reactions of metal ions Pearson, Ralph G. This article illustrates crystal field theory in studying substitution reactions of compounds of the metal ions. Pearson, Ralph G. J. Chem. Educ. 1961, 38, 164.
Crystal Field / Ligand Field Theory |
Metals |
Kinetics |
Aqueous Solution Chemistry
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The unraveling of geometric isomerism and tautomerism Ihde, Aaron J. Examines the work of Van't Hoff in unraveling isomerism due to carbon-carbon double bonds using fumaric and maleic acids as exemplars. Ihde, Aaron J. J. Chem. Educ. 1959, 36, 330.
Molecular Properties / Structure |
Stereochemistry |
Diastereomers
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Use of radioisotopes in the college chemistry laboratory Phillips, David; Maybury, Robert H. Provides experiments and experiences working with constructed Geiger counters and radioisotopes. Phillips, David; Maybury, Robert H. J. Chem. Educ. 1959, 36, 133.
Nuclear / Radiochemistry |
Isotopes |
Instrumental Methods |
Qualitative Analysis |
Kinetics
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Comparative organic chemistry: Carbon and silicon Wilk, I. J. Contrasts silicone chemistry with that of regular organic compounds. Wilk, I. J. J. Chem. Educ. 1957, 34, 463.
Covalent Bonding |
Ionic Bonding |
Mechanisms of Reactions |
Stereochemistry
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A simple kinetic model for single and consecutive first order reactions Kahn, Milton It is the purpose of this paper to describe an experiment whereby the validity of several kinetic relationships can be demonstrated without resorting to radioactive materials or actual chemical experimentation. Kahn, Milton J. Chem. Educ. 1957, 34, 148.
Kinetics |
Gases |
Equilibrium
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A notation for the study of certain stereochemical problems Newman, Melvin S. Newman introduces the projections of compounds containing two adjacent asymmetric carbons that would later bear his name. Newman, Melvin S. J. Chem. Educ. 1955, 32, 344.
Nomenclature / Units / Symbols |
Stereochemistry |
Molecular Properties / Structure |
Conformational Analysis |
Chirality / Optical Activity
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Nucleophilic substitution in aromatic systems Gillis, Richard G. Classifies and examines various categories of nucleophilic substitution in aromatic systems. Gillis, Richard G. J. Chem. Educ. 1955, 32, 296.
Nucleophilic Substitution |
Aromatic Compounds
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